Clinical Research Associate Sample CVs
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What makes a strong Clinical Research Associate CV
- List therapeutic areas: oncology, cardiovascular, CNS, infectious disease, rare disease
- Quantify sites monitored: number of sites, visits conducted, enrolment managed
- Highlight regulatory knowledge: ICH-GCP, 21 CFR Parts 11/50/54/56/312, MHRA, TGA, EMA
- Include SDV, data query resolution, safety reporting, and TMF management experience
- Mention CRO or sponsor experience and remote vs on-site monitoring capabilities
Key skills employers look for
Site Monitoring
On-site and remote SDV, eligibility review, informed consent, deviation management
Regulatory Compliance
ICH-GCP, 21 CFR, MHRA, TGA, EMA guidelines, audit readiness, CAPA management
Data Management
eCRF review, data query resolution, EDC systems (Medidata Rave, Oracle Inform, Veeva)
Safety & Documentation
SAE reporting, TMF maintenance, site file reconciliation, protocol deviation tracking
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